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1-Methyl-4-nitro-1H-pyrrolo[2,3-b]pyridine → 1-Methyl-1H-pyrrolo[2,3-b]pyridin-4-amine

HRID 2240234
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HRID 2240234 반응식
[CH3:1][N:2]1[C:6]2=[N:7][CH:8]=[CH:9][C:10]([N+:11]([O-])=O)=[C:5]2[CH:4]=[CH:3]1.[H][H]>C(O)C.C1COCC1.[Pt](=O)=O>[CH3:1][N:2]1[C:6]2[N:7]=[CH:8][CH:9]=[C:10]([NH2:11])[C:5]=2[CH:4]=[CH:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 593050251-Methyl-4-nitro-1H-pyrrolo[2,3-b]pyridineHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 552894121-Methyl-1H-pyrrolo[2,3-b]pyridin-4-amine

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 21873804Tetrahydrofuran ethanol용매

실험 절차

300 mg (1.69 mmol) of 1-methyl-4-nitro-1H-pyrrolo[2,3-b]pyridine are dissolved in a mixture of 20 ml of ethanol/THF (1:1). 38 mg (0.17 mmol) of platinum(IV) oxide are added, and the mixture is hydrogenated in a hydrogen atmosphere at atmospheric pressure overnight. The mixture is filtered through Celite and the solvent is removed under reduced pressure.

후처리

  1. filtrationThe mixture is filtered through Celite
  2. customthe solvent is removed under reduced pressure

출처 및 근거

ORD 기록
ord-0345f99d768646219f4c1f289a99ff1a
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07723347B2

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